Stereoselective Olefin Ring‐Opening Cross Metathesis Catalyzed by Molybdenum Imido Alkylidene N ‐Heterocyclic Carbene Complexes
Author:
Affiliation:
1. Institute of Polymer ChemistryUniversity of Stuttgart 70569 Stuttgart Germany
2. Institute of Textile Chemistry and Chemical Fibers (ITCF) Denkendorf 73770 Denkendorf Germany
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.201900979
Reference60 articles.
1. Regio- and Stereoselective Ring-Opening Cross-Metathesis. Rapid Entry into Functionalized Bicyclo[6.3.0] Ring Systems
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3. Catalytic Asymmetric Ring-Opening Metathesis/Cross Metathesis (AROM/CM) Reactions. Mechanism and Application to Enantioselective Synthesis of Functionalized Cyclopentanes
4. Highly Z- and Enantioselective Ring-Opening/Cross-Metathesis Reactions Catalyzed by Stereogenic-at-Mo Adamantylimido Complexes
5. Highly Z-Selective Metathesis Homocoupling of Terminal Olefins
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2. Effect of liquid confinement on regioselectivity in the hydrosilylation of alkynes with cationic Rh(i) N-heterocyclic carbene catalysts;Faraday Discussions;2023
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5. Cationic Molybdenum Imido Alkylidene N ‐Heterocyclic Carbene Complexes Confined in Mesoporous Silica: Tuning Transition States Towards Z ‐Selective Ring‐Opening Cross‐Metathesis;ChemCatChem;2022-10-13
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